Philips Respironics recalls Trilogy Evo O2 and LifeVent EVO2 models with serial numbers starting with H236054270DD5. Environmental debris can accumulate on the internal flow sensor, potentially causing inaccurate pressure delivery and patient harm if not addressed by a care provider.
Environmental debris may accumulate on the internal machine flow sensor causing partial occlusion which may impact accurate delivery of pressure, volume, or flow. A malfunction caused by this issue can result in patient harm up to hypoxemia if not addressed by the care provider.
Philips Respironics is recalling specific models of Trilogy Evo O2 and LifeVent EVO2 ventilators due to a risk that environmental debris can accumulate on the internal flow sensor. This may cause inaccurate delivery of pressure, volume, or flow, potentially leading to patient harm if not corrected by a healthcare provider.
Environmental debris can accumulate on the internal machine flow sensor, causing partial occlusion. This may lead to inaccurate delivery of pressure, volume, or flow, which can result in patient harm such as hypoxemia if not addressed by a healthcare provider.
Patients using the recalled Trilogy Evo O2 and LifeVent EVO2 ventilators with specific model numbers and serial numbers listed in the recall. Healthcare providers who manage these devices are most at risk.
Check if your device has model numbers DS2100X11B, IN2100X15B, IN2100X19, FX2100X15B, LA2100X15B, IA2100X15B, or serial numbers starting with H236054270DD5 through H257930929BA9 (and other listed serial numbers).
Your healthcare provider must address the issue to ensure accurate delivery of pressure, volume, or flow to prevent patient harm.
The affected models are Trilogy Evo O2 and LifeVent EVO2 with specific model numbers: DS2100X11B, IN2100X15B, IN2100X19, FX2100X15B, LA2100X15B, IA2100X15B, and serial numbers starting with H236054270DD5 through H257930929BA9 (and other listed serial numbers).
No, but your healthcare provider must address the issue to ensure accurate delivery of pressure, volume, or flow to prevent patient harm.
Check the model number and serial number on your device against the list of affected models and serial numbers provided in the recall notice.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-1650-2023 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-1650-2023 from Philips Respironics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
